| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:24955979-24956213 | Rare:85; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr8:24956588-24956697 | Common:1; Rare:27 | ||||
| chr8:24956730-24957020 | Common:2; Rare:59 | ||||
| chr8:25184250-25184580 | Common:2; Rare:77 | ||||
| chr8:25184612-25184809 | Common:1; Rare:64 | ||||
| chr8:25458675-25458966 | Common:4; Rare:89 | ||||
| chr8:26382916-26383110 | Rare:86 | ||||
| chr8:26383311-26383453 | Rare:40 | ||||
| chr8:26513849-26514207 | Common:1; Rare:78 | ||||
| chr8:26577037-26577148 | Rare:36 | ||||
| chr8:26577688-26578268 | Common:9; Rare:151 | ||||
| chr8:26578552-26578795 | Common:2; Rare:61 | ||||
| chr8:27311215-27311713 | Common:10; Rare:166 | ||||
| chr8:27490955-27491223 | Common:3; Rare:87 | ||||
| chr8:27614657-27614947 | Rare:99 |